首页> 外文期刊>Endocrinology >Roles of Rho guanosine 5'-triphosphatase A, Rho kinases, and extracellular signal regulated kinase (1/2) in prostaglandin E2-mediated migration of first-trimester human extravillous trophoblast.
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Roles of Rho guanosine 5'-triphosphatase A, Rho kinases, and extracellular signal regulated kinase (1/2) in prostaglandin E2-mediated migration of first-trimester human extravillous trophoblast.

机译:Rho鸟苷5'-三磷酸酶A,Rho激酶和细胞外信号调节激酶(1/2)在前列腺素E2介导的早孕人类绒毛外滋养层细胞迁移中的作用。

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摘要

Prostaglandin (PG) E(2) may regulate invasiveness of human placenta because we previously reported stimulation of migration of placental trophoblasts by PGE(2) acting through PGE receptor (EP)-1 and activating calpain. RhoA GTPase and its important effector Rho kinase (ROCK) have also been previously shown to regulate trophoblast migration. Using immortalized HTR-8/SVneo trophoblast cells and first-trimester human chorionic villus explant cultures on matrigel, we further examined the role of RhoA/ROCK and MAPK (ERK1/2) pathways on PGE(2)-mediated stimulation of trophoblast migration. Migration of cytotrophoblasts was shown to be inhibited by treatment of the trophoblast cell line and chorionic villus explants with either cell-permeable C3 transferase or selective RhoA small interfering RNA. These inhibitions were significantly mitigated by the addition of PGE(2), an EP1/EP3 agonist or an EP3/EP4 agonist, suggesting that RhoA plays an important role in trophoblast migration but may not be obligatory forPGE(2) action. Treatment of HTR-8/SVneo cells with nonselective ROCK inhibitor Y27632 or ROCK small interfering RNAs inhibited migration of these cells, which could not be rescued with PGE(2) or the other two EP agonists, suggesting the obligatory role of ROCK in PGE(2)-induced migratory response. Furthermore, U0126, an inhibitor of MAPK kinases MEK1 and MEK2, abrogated PGE(2)-induced migration of trophoblasts, and PGE(2) or the other two EP agonists stimulated ERK1/2 activation in trophoblasts, which was not abrogated by pretreatment with C3 transferase, indicating that ERK signaling pathway is an efficient alternate pathway for RhoA in PGE(2)-mediated migration of trophoblasts. These results suggest that ROCK and ERK1/2 play more important roles than RhoA in PGE(2)-mediated migration stimulation of first-trimester trophoblasts.
机译:前列腺素(PG)E(2)可能调节人类胎盘的侵袭性,因为我们先前曾报道过PGE(2)通过PGE受体(EP)-1和激活钙蛋白酶的作用刺激了胎盘滋养细胞的迁移。 RhoA GTPase及其重要效应子Rho激酶(ROCK)先前也已显示出调节滋养细胞迁移的作用。在基质胶上使用永生化的HTR-8 / SVneo滋养层细胞和早孕期人绒毛膜绒毛外植体培养物,我们进一步检查了RhoA / ROCK和MAPK(ERK1 / 2)途径在PGE(2)介导的滋养层迁移刺激中的作用。已显示通过使用可渗透细胞的C3转移酶或选择性RhoA小干扰RNA处理滋养细胞细胞系和绒毛膜绒毛外植体,可抑制滋养细胞的迁移。这些抑制作用通过添加PGE(2),EP1 / EP3激动剂或EP3 / EP4激动剂得以显着缓解,表明RhoA在滋养细胞迁移中起着重要作用,但对于PGE(2)作用可能不是必需的。用非选择性ROCK抑制剂Y27632或ROCK小干扰RNA处理HTR-8 / SVneo细胞可抑制这些细胞的迁移,而PGE(2)或其他两种EP激动剂无法挽救这些细胞的迁移,提示ROCK在PGE中的强制性作用( 2)引起的迁徙反应。此外,MAPK激酶MEK1和MEK2的抑制剂U0126消除了PGE(2)诱导的滋养细胞迁移,而PGE(2)或另外两个EP激动剂刺激了滋养细胞中的ERK1 / 2活化,但经预处理未消除C3转移酶,表明ERK信号通路是PGE(2)介导的滋养细胞迁移中RhoA的有效替代途径。这些结果表明,ROCK和ERK1 / 2在PGE(2)介导的孕早期滋养细胞的迁移刺激中起着比RhoA更重要的作用。

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